Elysium Pharmaceuticals Limited
FDA inspection history in VADODARA, India, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at VADODARA, India.
Cited most
Across all Elysium Pharmaceuticals Limited observations on file
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.188(b)(11)Batch production and control records1
- 21 CFR 211.194(a)Laboratory records1
- 21 CFR 211.48(a)Plumbing1
- 21 CFR 211.67(b)(6)Equipment cleaning and maintenance1
The complete Elysium Pharmaceuticals Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
VADODARA, India
One Form 483 · 2023 · 5 observations
Latest: Form 483, Jan 16, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-01-16 | 483 Form 483 | VADODARA, India | 5 | $99 |
Investigators on these documents
FEI number 3005183272 · most recent document Jan 16, 2023
About Elysium Pharmaceuticals Limited
How many FDA Form 483s has Elysium Pharmaceuticals Limited received?
FDA Intel has 1 Form 483 on file for Elysium Pharmaceuticals Limited; the most recent is dated Jan 16, 2023.
When was Elysium Pharmaceuticals Limited last inspected by FDA?
The most recent FDA inspection document on file for Elysium Pharmaceuticals Limited is a Form 483 dated Jan 16, 2023, for the site in VADODARA, India.
What did FDA cite at Elysium Pharmaceuticals Limited?
The regulations cited most in the observations on file for Elysium Pharmaceuticals Limited are 21 CFR 211.160(a) (General requirements), 1 time; 21 CFR 211.188(b)(11) (Batch production and control records), 1 time; 21 CFR 211.194(a) (Laboratory records), 1 time.